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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Kappa opioid agonists suppress chloroquine-induced scratching in mice.
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Kappa opioid agonists suppress chloroquine-induced scratching in mice.

机译:κ阿片类激动剂可抑制氯喹诱导的小鼠抓挠。

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摘要

Chemotherapy of malaria fever with chloroquine is often associated with generalized pruritus of unknown pathogenesis. This adverse side effect leads to diminished compliance. We report that chloroquine (1.25-40 mg/kg, s.c.) elicits dose-related, compulsive, and vigorous scratching in mice. This frenzied behavior is essentially abolished when the mice are pretreated s.c. or orally with nalfurafine (TRK-820), a centrally penetrating kappa opioid agonist. Peripheral kappa receptors are involved because chloroquine-induced scratching is also antagonized by the peripherally restricted kappa agonist, ICI 204,448: R,S-N-[2-(N-methyl-3,4-dichlorophenylacetamido)-2-(3-carboxyphenyl) ethyl]pyrrolidine. We propose that combination therapy for malaria with chloroquine and a kappa agonist (probably one targeting peripheral receptors) will lead to better treatment compliance because of a reduced incidence of pruritus.
机译:氯喹对疟疾热的化学疗法通常与未知发病机制的广泛性瘙痒症相关。这种不利的副作用导致顺从性下降。我们报道氯喹(1.25-40 mg / kg,s.c.)在小鼠中引起剂量相关的,强迫性的和剧烈的抓挠。当对小鼠进行s.c.预处理时,这种疯狂的行为基本上被消除了。或与中央渗透性κ阿片受体激动剂那氟拉芬(TRK-820)口服。涉及外围κ受体,因为氯喹诱导的刮擦也被外围受限的κ激动剂ICI 204,448所拮抗:R,SN- [2-(N-甲基-3,4-二氯苯基乙酰胺基)-2-(3-羧基苯基)乙基]吡咯烷。我们建议将氯喹与κ激动剂(可能是一种靶向外周受体)联合用于疟疾治疗,因为减少了瘙痒症,将导致更好的治疗依从性。

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